National Heart, Lung, and Blood Institute; Amended Notice of Meeting, 67050-67051 [2022-24203]
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67050
Federal Register / Vol. 87, No. 214 / Monday, November 7, 2022 / Notices
function of the agency, including
whether the information will have
practical utility; (2) The accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
Ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) Ways to minimize the
burden of the collection of information
on those who are to respond, including
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology.
Proposed Collection Title: NCI
Genomic Data Commons (GDC) Data
obtaining information from investigators
that: (1) would like to submit data about
their study into the GDC, (2) are
affiliated with studies that adhere to
GDC data submission conditions. The
benefits of the collection are that it
provides the needed information for
investigators to understand the types of
studies and data that the GDC supports
and that it provides a standard
mechanism for the GDC to assess
incoming data submission requests.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
50 hours.
Submission Request Form, 0925–0752,
Expiration Date 03/31/2023,
EXTENSION, National Cancer Institute
(NCI), National Institutes of Health
(NIH).
Need and Use of Information
Collection: The purpose of the NCI
Genomic Data Commons (GDC) Data
Submission Request Form is to provide
a vehicle for investigators to request the
submission of their cancer genomic data
into the GDC in support of data sharing.
The purpose is also to provide a
mechanism for the GDC Data
Submission Review Committee to
review and assess the data submission
request for applicability to the GDC
mission. The scope of the form involves
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Number of
respondents
Investigator ......................................................................................................
Total ..........................................................................................................
200
........................
Dated: November 2, 2022.
Diane Kreinbrink,
Project Clearance Liaison, National Cancer
Institute, National Institutes of Health.
[FR Doc. 2022–24186 Filed 11–4–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
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Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; RFA:
Countermeasures Against Chemical Threats
Exploratory/Developmental Projects.
Date: December 5, 2022.
Time: 8:30 a.m. to 8:00 p.m.
Agenda: To review and evaluate grant
applications.
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Place: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Jodie Michelle Fleming,
Ph.D., Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 812R,
Bethesda, MD 20892, (301) 867–5309,
flemingjm@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Small
Business: Microbial Vaccine Development.
Date: December 5–6, 2022.
Time: 10:00 a.m. to 8:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Subhamoy Pal, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Bethesda, MD
20892, (301) 594–0926, subhamoy.pal@
nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel;
Fellowships: Oncology.
Date: December 6–7, 2022.
Time: 10:00 a.m. to 8:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Nywana Sizemore, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6189,
MSC 7804, Bethesda, MD 20892, 301–408–
9916, sizemoren@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel;
Epigenomics of Neurodevelopment.
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Number of
responses per
respondent
1
200
Average time
per response
(in hours)
Total annual
burden hour
15/60
........................
50
50
Date: December 6, 2022.
Time: 2:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Mary G Schueler, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5214,
MSC 7846, Bethesda, MD 20892, 301–915–
6301, marygs@csr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: November 2, 2022.
David W. Freeman,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2022–24204 Filed 11–4–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
Institute; Amended Notice of Meeting
Notice is hereby given of a change in
the meeting of the Sleep Disorders
Research Advisory Board, December 01,
2022, 12 p.m. to December 01, 2022, 4
p.m., National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD, 20892 which was
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Federal Register / Vol. 87, No. 214 / Monday, November 7, 2022 / Notices
published in the Federal Register on
November 01, 2022, 87 FR 65786.
Meeting is being amended to change
the meeting time from 12 p.m. to 4 p.m.
to 12 p.m. to 5 p.m. Also to change the
agenda from, ‘‘The purpose of this
meeting is to update the Advisory Board
and public stakeholders on the research
agenda across NIH for the upcoming
fiscal year, and the activities of
professional societies.’’ to ‘‘The purpose
of this meeting is to discuss with the
Advisory Board timely research
opportunities in sleep and circadian
biology. Updates on the research agenda
across the NIH for the upcoming fiscal
year and the activities of professional
societies will be provided to all
stakeholders.’’ The meeting is open to
the public.
Dated: November 2, 2022.
David W. Freeman,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2022–24203 Filed 11–4–22; 8:45 am]
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DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
[Docket No. FR–6331–N–08]
Public Interest De Minimis, Small
Grants, and Minor Components Waiver
of Build America, Buy America
Provisions as Applied to Certain
Recipients of HUD Federal Financial
Assistance
Office of the Secretary, U.S.
Department of Housing and Urban
Development (HUD).
ACTION: Notice.
AGENCY:
In accordance with the Build
America, Buy America Act (‘‘BABA’’ or
‘‘the Act’’) this notice advises that HUD
is proposing a departmentwide public
interest de minimis, Small Grants, and
Minor Components waiver to the Buy
America Domestic Content Procurement
Preference (‘‘Buy America Preference,’’
or ‘‘BAP’’) as applied to the iron, steel,
manufactured products, and
construction materials requirement of
the Act for recipients of Federal
Financial Assistance. For the purposes
of this proposed waiver, HUD is
proposing to waive the application of
the BAP for infrastructure projects
whose total cost is an amount equal to
or less than the Simplified acquisition
threshold, which is currently $250,000.
HUD is also proposing to waive the
application of the BAP for all Small
Grants of Federal Financial Assistance
that are equal to or below the Simplified
acquisition threshold, which is
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SUMMARY:
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currently $250,000. Additionally, HUD
is proposing to waive the application of
the BAP for Minor Components of an
infrastructure project, such that a
cumulative total of no more than a total
of 5 percent of the total cost of the iron,
steel, manufactured products, and
construction materials used in and
incorporated into the infrastructure
project, up to a maximum of $1 million.
In accordance with the Act, HUD has
found that such proposed De Minimis,
Small Grants and Minor Components
waivers are in the public interest. The
waiver will assist HUD and its grantees
and funding recipients in preventing
immediate delays to critically important
projects that serve to ensuring the safety
and health of HUD constituents and
continuing to provide economic
opportunity through housing and
community development projects.
Moreover, this waiver will assist HUD
in working to strengthen the housing
market to bolster the economy and
protect consumers, meet the need for
quality affordable rental homes, utilize
housing as a platform for improving
quality of life, and build inclusive and
sustainable communities free from
discrimination.
DATES: HUD published this proposed
waiver on its website on October 31,
2022. Comments on the proposed
waiver set out in this document are due
on or before November 15, 2022.
ADDRESSES: Interested persons are
invited to submit comments on this
proposed general applicability waiver.
Copies of all comments submitted are
available for inspection and
downloading at www.regulations.gov.
To receive consideration as public
comments, comments must be
submitted through one of two methods,
specified below. All submissions must
refer to the above docket number and
title.
1. Electronic Submission of
Comments. Interested persons may
submit comments electronically through
the Federal eRulemaking Portal at
www.regulations.gov.
HUD strongly encourages commenters
to submit comments electronically.
Electronic submission of comments
allows the commenter maximum time to
prepare and submit a comment, ensures
timely receipt by HUD, and enables
HUD to make them immediately
available to the public. Comments
submitted electronically through the
www.regulations.gov website can be
viewed by other commenters and
interested members of the public.
Commenters should follow the
instructions provided on that site to
submit comments electronically.
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67051
2. Submission of Comments by Mail.
Comments may be submitted by mail to
the Regulations Division, Office of
General Counsel, Department of
Housing and Urban Development, 451
7th Street SW, Room 10276,
Washington, DC 20410–0500.
No Facsimile Comments. Facsimile
(FAX) comments will not be accepted.
3. Public Inspection of Comments. All
properly submitted comments and
communications submitted to HUD will
be available for public inspection and
copying between 8:00 a.m. and 5:00
p.m. weekdays at the above address.
Due to security measures at the HUD
Headquarters building, an advance
appointment to review the submissions
must be scheduled by calling the
Regulations Division at (202) 708–3055
(this is not a toll-free number).
FOR FURTHER INFORMATION CONTACT:
Joseph Carlile, Department of Housing
and Urban Development, 451 Seventh
Street SW, Room 10226, Washington,
DC 20410–5000, at (202) 402–7082 (this
is not a toll-free number). HUD
welcomes and is prepared to receive
calls from individuals who are deaf or
hard of hearing, as well as individuals
with speech and communication
disabilities. To learn more about how to
make an accessible telephone call,
please visit https://www.fcc.gov/
consumers/guides/telecommunicationsrelay-service-trs. HUD encourages
submission of questions about this
document be sent to
BuildAmericaBuyAmerica@hud.gov.
SUPPLEMENTARY INFORMATION:
I. Build America, Buy America
The Build America, Buy America Act
(‘‘BABA’’ or ‘‘the Act’’) was enacted on
November 15, 2021, as part of the
Infrastructure Investment and Jobs Act
(IIJA). Public Law 117–58. The Act
establishes a domestic content
procurement preference, the BAP, for
Federal infrastructure programs. Section
70914(a) of the Act establishes that no
later than 180 days after the date of
enactment, HUD must ensure that none
of the funds made available for
infrastructure projects may be obligated
by the Department unless it has taken
steps to ensure that the iron, steel,
manufactured products, and
construction materials used in a project
are produced in the United States. In
section 70912, the Act further defines a
project to include ‘‘the construction,
alteration, maintenance, or repair of
infrastructure in the United States’’ and
includes within the definition of
infrastructure those items traditionally
included along with buildings and real
property. Thus, starting May 14, 2022,
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Agencies
[Federal Register Volume 87, Number 214 (Monday, November 7, 2022)]
[Notices]
[Pages 67050-67051]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-24203]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood Institute; Amended Notice of
Meeting
Notice is hereby given of a change in the meeting of the Sleep
Disorders Research Advisory Board, December 01, 2022, 12 p.m. to
December 01, 2022, 4 p.m., National Institutes of Health, Rockledge II,
6701 Rockledge Drive, Bethesda, MD, 20892 which was
[[Page 67051]]
published in the Federal Register on November 01, 2022, 87 FR 65786.
Meeting is being amended to change the meeting time from 12 p.m. to
4 p.m. to 12 p.m. to 5 p.m. Also to change the agenda from, ``The
purpose of this meeting is to update the Advisory Board and public
stakeholders on the research agenda across NIH for the upcoming fiscal
year, and the activities of professional societies.'' to ``The purpose
of this meeting is to discuss with the Advisory Board timely research
opportunities in sleep and circadian biology. Updates on the research
agenda across the NIH for the upcoming fiscal year and the activities
of professional societies will be provided to all stakeholders.'' The
meeting is open to the public.
Dated: November 2, 2022.
David W. Freeman,
Program Analyst, Office of Federal Advisory Committee Policy.
[FR Doc. 2022-24203 Filed 11-4-22; 8:45 am]
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